A rare lung disorder characterized by the filling of the pulmonary alveoli with proteinaceous material which stains positive with periodic acid-Schiff stain. It may be idiopathic or secondary due to hematologic malignancies or the inhalation of mineral dusts. Signs and symptoms include dyspnea, cough and low grade fever. [ NCIT:C85037 ]

This is just here as a test because I lose it

Term information

database cross reference
  • NCIT:C85037 (MONDO:equivalentTo)
  • DOID:12120 (MONDO:equivalentTo)
  • Reactome:R-HSA-5683826
  • SCTID:10501004 (MONDO:equivalentTo)
  • ICD10:J84.01 (DOID:12120)
  • ICD9:516.0 (i2s)
  • MESH:D011649 (MONDO:equivalentTo)
  • UMLS:C0034050 (NCIT:C85037)
abbreviation
PAP [ MONDO:cjm ]

definition

A rare lung disorder characterized by the filling of the pulmonary alveoli with proteinaceous material which stains positive with periodic acid-Schiff stain. It may be idiopathic or secondary due to hematologic malignancies or the inhalation of mineral dusts. Signs and symptoms include dyspnea, cough and low grade fever.

exactMatch

http://purl.obolibrary.org/obo/DOID_12120

http://linkedlifedata.com/resource/umls/id/C0034050

http://identifiers.org/mesh/D011649

http://identifiers.org/snomedct/10501004

http://purl.obolibrary.org/obo/NCIT_C85037

has exact synonym

pulmonary alveolar proteinosis

id

MONDO:0001437